Skip to main content
OpenTrials
Completed

NCT Number: NCT00719966

Effect of Aromatase Inhibitor Therapy on Blood Vessel Function in Postmenopausal Women With Breast Cancer

RATIONALE: Aromatase inhibitor therapy is used in treating postmenopausal women who have hormone-dependent breast cancer. It is not yet known what effect aromatase inhibitor therapy has on blood vessel function.

PURPOSE: This clinical trial is studying the effect of aromatase inhibitor therapy on blood vessel function in postmenopausal women with breast cancer.

Completed

Looking for future studies?

Notify Me

Key information

About this study

OBJECTIVES:

  • Determine the effect of adjuvant aromatase inhibitor therapy on endothelial function in postmenopausal women with breast cancer.

OUTLINE: This is a multicenter study. Patients are assigned to 1 of 2 treatment groups according to breast cancer hormone-receptor status (positive vs negative).

  • Group 1 (hormone receptor-positive): Patients receive aromatase inhibition therapy for up to 6 months in the absence of unacceptable toxicity.
  • Group 2 (hormone receptor-negative): Patients do not receive adjuvant treatment.

Endothelial function is measured in both groups at baseline and at follow up by the room temperature peripheral arterial tonometry (RT-PAT) index using the EndoPAT method.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

DISEASE CHARACTERISTICS:

  • Diagnosis of breast cancer
  • Ductal carcinoma in situ (DCIS) allowed provided the patient will not receive tamoxifen as part of treatment for their cancer
  • May not have had a prior mastectomy with requirement for mastectomy of the contralateral breast
  • No requirement for axillary lymph node dissection with a history of contralateral mastectomy and/or contralateral axillary lymph node dissection
  • Hormone receptor status meeting 1 of the following criteria:
  • Hormone receptor negative and not eligible for aromatase inhibitor therapy (AI)
  • Hormone receptor positive and are not receiving an AI

PATIENT CHARACTERISTICS:

  • Postmenopausal
  • No known or symptomatic coronary artery disease
  • No significant co-morbidities, including any of the following conditions:
  • Active renal or hepatic disease
  • Known uncontrolled and/or untreated peripheral arterial disease
  • Uncontrolled and/or untreated hypertension
  • Uncontrolled and/or untreated diabetes
  • Uncontrolled and/or untreated hyperlipidemia

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • More than 7 days since prior hormone replacement therapy or hormone-based contraception
  • More than 12 months since prior and no concurrent tamoxifen or aromatase inhibitor therapy for this disease
  • More than 12 months since prior and no concurrent chemotherapy for this disease
  • No prior bilateral mastectomy

Treatment and study plan

Anastrozole

Drug

Patients receive aromatase inhibition therapy.

Exemestane

Drug

Patients receive aromatase inhibition therapy.

letrozole

Drug

Patients receive aromatase inhibition therapy.

assessment of therapy complications

Procedure

Endothelial function is measured

Primary outcomes

  1. Endothelial dysfunction as a result of aromatase inhibitor therapy

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

Effect of Aromatase Inhibitor Therapy for Breast Cancer on Endothelial Function

Important dates

Study start
2008
Primary completion
2013
Study completion
2020
First posted
Jul 22, 2008
Registry last updated
Jan 2, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.